SE-ATLAS

Hypertrophic cardiomyopathy due to intensive athletic training Familial dilated cardiomyopathy Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Mucopolysaccharidosis type 2, attenuated form Dilated cardiomyopathy Neuromuscular disease with dilated cardiomyopathy Kidney tubulopathy-dilated cardiomyopathy syndrome Mitochondrial disease with dilated cardiomyopathy Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant Syndrome associated with dilated cardiomyopathy Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease Sensorineural deafness with dilated cardiomyopathy Beckwith-Wiedemann syndrome due to NSD1 mutation Jervell and Lange-Nielsen syndrome Non-familial dilated cardiomyopathy Familial restrictive cardiomyopathy Restrictive cardiomyopathy Autosomal dominant Emery-Dreifuss muscular dystrophy Lysosomal disease with restrictive cardiomyopathy MELAS Autosomal recessive Emery-Dreifuss muscular dystrophy MERRF Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease X-linked Emery-Dreifuss muscular dystrophy Marfan syndrome Genetic cardiac rhythm disease Acyl-CoA dehydrogenase 9 deficiency Long chain acyl-CoA dehydrogenase deficiency Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3 Alström syndrome Primary hypereosinophilic syndrome Mucopolysaccharidosis type 2 1p36 deletion syndrome HEC syndrome Glycogen storage disease due to acid maltase deficiency, late-onset Dilated cardiomyopathy with ataxia Unclassified cardiomyopathy Becker muscular dystrophy Secondary hypereosinophilic syndrome Familial abdominal aortic aneurysm Friedreich ataxia Early-onset myopathy with fatal cardiomyopathy Nathalie syndrome Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome Barth syndrome Beckwith-Wiedemann syndrome Loeys-Dietz syndrome Brugada syndrome Noonan syndrome-like disorder with loose anagen hair Ocular anomalies-axonal neuropathy-developmental delay syndrome Familial isolated dilated cardiomyopathy PGM1-CDG Non-familial rare disease with dilated cardiomyopathy Familial bicuspid aortic valve Systemic primary carnitine deficiency Carnitine-acylcarnitine translocase deficiency Multiple acyl-CoA dehydrogenase deficiency Very long chain acyl-CoA dehydrogenase deficiency Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome Andersen-Tawil syndrome Systemic sclerosis CREST syndrome Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Eosinophilic granulomatosis with polyangiitis Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion Fukutin-related limb-girdle muscular dystrophy R13 Delta-sarcoglycan-related limb-girdle muscular dystrophy R6 Sinoatrial node dysfunction and deafness Familial aortic dissection Mitochondrial trifunctional protein deficiency Diffuse cutaneous systemic sclerosis Sino-auricular heart block Limited cutaneous systemic sclerosis 46,XY complete gonadal dysgenesis Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency Adult polyglucosan body disease Inherited arrhythmogenic cardiomyopathy Familial thoracic aortic aneurysm and aortic dissection Kombinierter Defekt der oxidativen Phosphorylierung Typ 17 Long-QT-Syndrom, familiäres Emery-Dreifuss Muskeldystrophie Duchenne- und Becker-Muskeldystrophie Gliedergürtelmuskeldystrophie, autosomal-dominante, Typ 1B Kardiomyopathie, hypertrophe mitochondriale, mit Laktatazidose durch MTO1-Mangel Arterial-Tortuosity-Syndrom Myotone Dystrophie Steinert Syndrom der chronischen atrialen und intestinalen Rhythmusstörung Wildtyp-ATTR-Amyloidose Glykogenose durch LAMP-2-Mangel Sarkoidose Ehlers-Danlos-Syndrom, vaskulärer Typ Hurler-Syndrom Multipler Acyl-CoA-Dehydrogenase-Mangel, milder Typ Hurler-Scheie-Syndrom Multipler Acyl-CoA-Dehydrogenase-Mangel, schwerer neonataler Typ Marfan-Syndrom Typ 1 Marfan-Syndrom Typ 2 Endomyokardfibrose, tropische Löffler-Endokarditis Kammerflimmern, idiopathisches (nicht Brugada-Typ) Infantile hypertrophe Kardiomyopathie durch MRPL44-Mangel Isobutyryl-CoA-Dehydrogenasemangel Aneurysma-Osteoarthritis-Syndrom Herz-Hand-Syndrom Typ 3 X-chromosomale Intelligenzminderung-Kardiomegalie-kongestive Herzinsuffizienz-Syndrom Vorhofstillstand Kardiomyopathie-Katarakt-Hüftwirbelsäulenerkrankung-Syndrom DPM3-CDG Fabry-Syndrom Mitochondriale DNA-assoziierte Kardiomyopathie mit Hörverlust Uhl-Anomalie Glykogenose Typ 2, infantile Form Vorhofflimmern, familiäres Amyloidose, lokalisierte primäre Fukosidose Herz-Hand-Syndrom, slowenischer Typ Familiäre progressive kardiale Reizleitungsstörungen Glykogenose Typ 2 Gliedergürtelmuskeldystrophie, autosomal-rezessive, Typ 2W Brachydaktylie mit langem Daumen Holt-Oram-Syndrom Sick-Sinus-Syndrom, familiäres Torsade de pointes mit kurzem Kopplungsintervall Glykogenose Typ 4, nonprogressive hepatische Form Hypertrophe Kardiomyopathie mit Nierenanomalien durch mitochondriale DNA-Mutation Seltene Kardiomyopathie Glykogenose durch Glykogen-Branching-Enzym-Mangel, fatale perinatale neuromuskuläre Form Gliedergürtelmuskeldystrophie, autosomal-rezessive, Typ 2X Glykogenose durch Glykogen-Branching-Enzym-Mangel, kongenitale neuromuskuläre Form Noonan-ähnliches Syndrom mit juveniler myelomonozytischer Leukämie AA-Amyloidose Atriumseptumdefekt mit atrio-ventrikulären Reizleitungsstörungen Kardiomyopathie, histiozytoide Gaucher-Krankheit Typ 1 Mikrozephalie - Kardiomyopathie Glykogenose durch Glykogen-Branching-Enzym-Mangel, infantile neuromuskuläre Form Kearns-Sayre-Syndrom Endocardial fibroelastosis Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome Multisystemic smooth muscle dysfunction syndrome Congenital disorder of glycosylation with dilated cardiomyopathy Lysosomal disease with hypertrophic cardiomyopathy Mitochondrial disease with hypertrophic cardiomyopathy Familial isolated restrictive cardiomyopathy Noonan syndrome with multiple lentigines DK1-CDG Cardiomyopathy-hypotonia-lactic acidosis syndrome Non-familial hypertrophic cardiomyopathy Hypereosinophilic syndrome Mucopolysaccharidosis type 2, severe form Peripartum cardiomyopathy Inherited isolated arrhythmogenic cardiomyopathy Duchenne muscular dystrophy Ehlers-Danlos syndrome with periventricular heterotopia Desminopathy Lymphocytic hypereosinophilic syndrome Leber hereditary optic neuropathy Combined oxidative phosphorylation defect type 23 Beta-mannosidosis Beta-sarcoglycan-related limb-girdle muscular dystrophy R4 Polyglucosan body myopathy type 1 Non-familial restrictive cardiomyopathy Noonan syndrome Congenital heart block Idiopathic giant cell myocarditis Romano-Ward syndrome Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome Idiopathic hypereosinophilic syndrome Familial dilated cardiomyopathy with conduction defect due to LMNA mutation Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers Beckwith-Wiedemann syndrome due to CDKN1C mutation His bundle tachycardia Alpha-B crystallin-related late-onset myopathy Beckwith-Wiedemann syndrome due to 11p15 microdeletion Catecholaminergic polymorphic ventricular tachycardia Limited systemic sclerosis Pseudoxanthoma elasticum Carvajal syndrome Timothy syndrome Neonatal Marfan syndrome Cardiofaciocutaneous syndrome Heart-hand syndrome type 2 Primary systemic amyloidosis Lown-Ganong-Levine syndrome Beckwith-Wiedemann syndrome due to 11p15 microduplication Rare disease with thoracic aortic aneurysm and aortic dissection Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5 Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Glycogen storage disease due to glycogen debranching enzyme deficiency Glycogen storage disease due to glycogen branching enzyme deficiency Diabetic embryopathy Leber plus disease Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form Familial short QT syndrome Rare familial disorder with hypertrophic cardiomyopathy Glycogen storage disease due to muscle and heart glycogen synthase deficiency Naxos disease McLeod neuroacanthocytosis syndrome Cirrhotic cardiomyopathy Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 AL amyloidosis Erythrokeratodermia-cardiomyopathy syndrome Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form ATTRV122I amyloidosis Gaucher disease type 3 Vici syndrome Tako-Tsubo cardiomyopathy Rare hypertrophic cardiomyopathy Glycogen storage disease with hypertrophic cardiomyopathy Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form Fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy Left ventricular noncompaction Syndrome associated with hypertrophic cardiomyopathy Costello syndrome